# K182646: Vitreq disposable laser probes, light fibers and Chandelier

- Pathway: 510(k) (Traditional)
- Applicant: VitreQ BV
- Decided: May 1, 2019 after 219 days
- Product code: HQB (Photocoagulator And Accessories)
- Device class: 2
- Regulation: 21 CFR 886.4690
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 5 generations back to K954307 (1995). 15 ancestors in all.
No later device cites it as a predicate yet.
0 of 16 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K121187: Katalyst Laser Probes, Katalyst Illuminated Laser Probes, Katalyst Surgical, LLC (2012) Summary page 4.
- K151604: 23ga Chandelier Illuminator, 25ga Chandelier Illuminator, Peregrine Surgical, Ltd. (2015) Summary page 4.

## Indications for use
VitreQ Disposable Laser Probes, 90° Directional Laser Probes and 90° Directional Illuminated Laser Probes are intended for use in vitreoretinal surgery to perform endo-ocular laser photocoagulation treatments at operating wavelengths of 500nm to 900nm. The 90° Directional Illuminated Laser Probes, Light Fibers and Chandelier are for illumination during ophthalmic surgery and should only be used with the light wavelength range of 425nm to 700nm.

Source page: https://510kreport.com/device/K182646
Methodology: https://510kreport.com/methodology